Clinical Project Manager

Lead and manage all aspects of clinical trials from initiation through closeout, ensuring compliance with regulatory requirements, SOPs, timelines, and budget. Develop project plans, oversee resource allocation, and serve as the primary liaison between internal teams, clinical research sites, CROs, and vendors. Lead cross-functional meetings, coordinate study activities including site selection and monitoring, and track metrics to prepare status reports. Support regulatory and audit readiness by contributing to study documentation and inspection preparation. Participate in protocol development, CRF design, and review of key trial documents. Monitor progress against timelines and budget while proactively identifying risks and implementing mitigation strategies. Oversee vendor performance and manage contract deliverables for external partners.